meddevicedb.com FDA Device Reference

Tablo Console with Wireless Capability

K150880 Class II Special
Decision Date
2015-05-01
Sponsor / Applicant
Outset Medical

Technical Specification

510(k) Submission ID K150880
Product Code KDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5860
Decision Date 2015-05-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tablo Console with Wireless Capability received FDA 510(k) clearance under submission number K150880, sponsored by Outset Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2015-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code KDI and 21 CFR 876.5860, within the Gastroenterology, Urology review panel as a Class II device.